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/ Gi View , Ltd.
Gi View , Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K230588
Aer-O-Scope Colonoscope System
August 17, 2023
K161791
Aer-O-Scope Colonoscope System
August 11, 2016
K141286
AER-O-SCOPE COLONOSCOPE SYSTEM
September 30, 2014